US4680415A - Intermediates for 7-fluoro dihydro PGI compounds - Google Patents
Intermediates for 7-fluoro dihydro PGI compounds Download PDFInfo
- Publication number
- US4680415A US4680415A US06/885,993 US88599386A US4680415A US 4680415 A US4680415 A US 4680415A US 88599386 A US88599386 A US 88599386A US 4680415 A US4680415 A US 4680415A
- Authority
- US
- United States
- Prior art keywords
- alpha
- fluoro
- compound
- oxy
- dimethylsilyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000543 intermediate Substances 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 128
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 45
- 239000001257 hydrogen Substances 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- KXGVEGMKQFWNSR-LLQZFEROSA-N deoxycholic acid Chemical compound C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 KXGVEGMKQFWNSR-LLQZFEROSA-N 0.000 claims description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- 125000001153 fluoro group Chemical group F* 0.000 claims description 14
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 10
- 230000003287 optical effect Effects 0.000 claims description 9
- 150000002431 hydrogen Chemical group 0.000 claims description 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims 2
- 125000005103 alkyl silyl group Chemical group 0.000 claims 1
- 210000001772 blood platelet Anatomy 0.000 abstract description 19
- 230000002744 anti-aggregatory effect Effects 0.000 abstract description 7
- 229920006395 saturated elastomer Polymers 0.000 abstract description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 102
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 90
- 239000000203 mixture Substances 0.000 description 73
- 239000000243 solution Substances 0.000 description 51
- 238000006243 chemical reaction Methods 0.000 description 44
- 239000002253 acid Substances 0.000 description 30
- 239000002904 solvent Substances 0.000 description 24
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 22
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 22
- -1 -halo PGI2 derivatives Chemical class 0.000 description 21
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 21
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 20
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 20
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 18
- 125000003118 aryl group Chemical group 0.000 description 16
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 15
- 239000004615 ingredient Substances 0.000 description 15
- 210000004623 platelet-rich plasma Anatomy 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000003814 drug Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 14
- 150000003839 salts Chemical class 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 13
- 229920001214 Polysorbate 60 Polymers 0.000 description 13
- 238000004519 manufacturing process Methods 0.000 description 13
- 239000003208 petroleum Substances 0.000 description 13
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 229940079593 drug Drugs 0.000 description 12
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 12
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 12
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 12
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 12
- HVAUUPRFYPCOCA-AREMUKBSSA-N 2-O-acetyl-1-O-hexadecyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCOC[C@@H](OC(C)=O)COP([O-])(=O)OCC[N+](C)(C)C HVAUUPRFYPCOCA-AREMUKBSSA-N 0.000 description 11
- 108010003541 Platelet Activating Factor Proteins 0.000 description 11
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 11
- 239000000741 silica gel Substances 0.000 description 11
- 229910002027 silica gel Inorganic materials 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 229940114079 arachidonic acid Drugs 0.000 description 10
- 235000021342 arachidonic acid Nutrition 0.000 description 10
- 239000006071 cream Substances 0.000 description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 10
- 102000008186 Collagen Human genes 0.000 description 9
- 108010035532 Collagen Proteins 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 101000956368 Trittame loki CRISP/Allergen/PR-1 Proteins 0.000 description 9
- 229920001436 collagen Polymers 0.000 description 9
- 235000019441 ethanol Nutrition 0.000 description 9
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 8
- 229910052783 alkali metal Inorganic materials 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 8
- IVOMOUWHDPKRLL-KQYNXXCUSA-N Cyclic adenosine monophosphate Chemical compound C([C@H]1O2)OP(O)(=O)O[C@H]1[C@@H](O)[C@@H]2N1C(N=CN=C2N)=C2N=C1 IVOMOUWHDPKRLL-KQYNXXCUSA-N 0.000 description 7
- 238000003776 cleavage reaction Methods 0.000 description 7
- 239000012230 colorless oil Substances 0.000 description 7
- 150000002148 esters Chemical group 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 235000019271 petrolatum Nutrition 0.000 description 7
- 230000007017 scission Effects 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 230000000699 topical effect Effects 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 6
- 239000004264 Petrolatum Substances 0.000 description 6
- IVOMOUWHDPKRLL-UHFFFAOYSA-N UNPD107823 Natural products O1C2COP(O)(=O)OC2C(O)C1N1C(N=CN=C2N)=C2N=C1 IVOMOUWHDPKRLL-UHFFFAOYSA-N 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 6
- 238000004220 aggregation Methods 0.000 description 6
- 230000002776 aggregation Effects 0.000 description 6
- 229910052786 argon Inorganic materials 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 229960000541 cetyl alcohol Drugs 0.000 description 6
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 6
- 229940095074 cyclic amp Drugs 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 239000008101 lactose Substances 0.000 description 6
- 235000019359 magnesium stearate Nutrition 0.000 description 6
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 6
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 6
- 229960002216 methylparaben Drugs 0.000 description 6
- 229940066842 petrolatum Drugs 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 6
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 6
- 229940113124 polysorbate 60 Drugs 0.000 description 6
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 6
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 6
- 229960003415 propylparaben Drugs 0.000 description 6
- KAQKFAOMNZTLHT-OZUDYXHBSA-N prostaglandin I2 Chemical compound O1\C(=C/CCCC(O)=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)CCCCC)[C@H](O)C[C@@H]21 KAQKFAOMNZTLHT-OZUDYXHBSA-N 0.000 description 6
- 239000008213 purified water Substances 0.000 description 6
- 159000000000 sodium salts Chemical class 0.000 description 6
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 5
- 229960000583 acetic acid Drugs 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 150000001340 alkali metals Chemical class 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 125000001033 ether group Chemical group 0.000 description 5
- 229940075507 glyceryl monostearate Drugs 0.000 description 5
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- 150000007524 organic acids Chemical class 0.000 description 5
- 239000000825 pharmaceutical preparation Substances 0.000 description 5
- 150000003815 prostacyclins Chemical class 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000003381 stabilizer Substances 0.000 description 5
- 229920003084 Avicel® PH-102 Polymers 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 229920000881 Modified starch Polymers 0.000 description 4
- 239000004368 Modified starch Substances 0.000 description 4
- LQZMLBORDGWNPD-UHFFFAOYSA-N N-iodosuccinimide Chemical compound IN1C(=O)CCC1=O LQZMLBORDGWNPD-UHFFFAOYSA-N 0.000 description 4
- 239000013543 active substance Substances 0.000 description 4
- 230000036772 blood pressure Effects 0.000 description 4
- 239000002775 capsule Substances 0.000 description 4
- 239000007963 capsule composition Substances 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 238000010828 elution Methods 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000007903 gelatin capsule Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 235000019426 modified starch Nutrition 0.000 description 4
- 231100000252 nontoxic Toxicity 0.000 description 4
- 230000003000 nontoxic effect Effects 0.000 description 4
- 230000003389 potentiating effect Effects 0.000 description 4
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- BLIQUJLAJXRXSG-UHFFFAOYSA-N 1-benzyl-3-(trifluoromethyl)pyrrolidin-1-ium-3-carboxylate Chemical compound C1C(C(=O)O)(C(F)(F)F)CCN1CC1=CC=CC=C1 BLIQUJLAJXRXSG-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 229940126062 Compound A Drugs 0.000 description 3
- 229920002261 Corn starch Polymers 0.000 description 3
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 description 3
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 239000008120 corn starch Substances 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 229960001123 epoprostenol Drugs 0.000 description 3
- 239000012025 fluorinating agent Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000005457 ice water Substances 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 239000002674 ointment Substances 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
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- 229910052697 platinum Inorganic materials 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 3
- 238000011200 topical administration Methods 0.000 description 3
- 239000005051 trimethylchlorosilane Substances 0.000 description 3
- HUHXLHLWASNVDB-UHFFFAOYSA-N 2-(oxan-2-yloxy)oxane Chemical compound O1CCCCC1OC1OCCCC1 HUHXLHLWASNVDB-UHFFFAOYSA-N 0.000 description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 2
- GUBGYTABKSRVRQ-DCSYEGIMSA-N Beta-Lactose Chemical compound OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-DCSYEGIMSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
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- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- QAQJMLQRFWZOBN-LAUBAEHRSA-N L-ascorbyl-6-palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(O)=C1O QAQJMLQRFWZOBN-LAUBAEHRSA-N 0.000 description 2
- 239000011786 L-ascorbyl-6-palmitate Substances 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- 229910017917 NH4 Cl Inorganic materials 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 235000010385 ascorbyl palmitate Nutrition 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005661 deetherification reaction Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 238000007907 direct compression Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000003937 drug carrier Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 238000010931 ester hydrolysis Methods 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 239000012259 ether extract Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 230000002140 halogenating effect Effects 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
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- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
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- 239000000460 chlorine Substances 0.000 description 1
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- 239000012043 crude product Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- HWLZQESIRAGTAT-UHFFFAOYSA-N cyclopenta[b]furan-2-one Chemical compound C1=CC2=CC(=O)OC2=C1 HWLZQESIRAGTAT-UHFFFAOYSA-N 0.000 description 1
- 238000006704 dehydrohalogenation reaction Methods 0.000 description 1
- 125000005265 dialkylamine group Chemical group 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002084 enol ethers Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- DECIPOUIJURFOJ-UHFFFAOYSA-N ethoxyquin Chemical compound N1C(C)(C)C=C(C)C2=CC(OCC)=CC=C21 DECIPOUIJURFOJ-UHFFFAOYSA-N 0.000 description 1
- 235000019285 ethoxyquin Nutrition 0.000 description 1
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- 239000012530 fluid Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
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- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
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- 230000005484 gravity Effects 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- XUPLQGYCPSEKNQ-UHFFFAOYSA-H hexasodium dioxido-oxo-sulfanylidene-lambda6-sulfane Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]S([O-])(=O)=S.[O-]S([O-])(=O)=S.[O-]S([O-])(=O)=S XUPLQGYCPSEKNQ-UHFFFAOYSA-H 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
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- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
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- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
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- YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 1
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- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- SGUKUZOVHSFKPH-YNNPMVKQSA-N prostaglandin G2 Chemical compound C1[C@@H]2OO[C@H]1[C@H](/C=C/[C@@H](OO)CCCCC)[C@H]2C\C=C/CCCC(O)=O SGUKUZOVHSFKPH-YNNPMVKQSA-N 0.000 description 1
- YIBNHAJFJUQSRA-YNNPMVKQSA-N prostaglandin H2 Chemical compound C1[C@@H]2OO[C@H]1[C@H](/C=C/[C@@H](O)CCCCC)[C@H]2C\C=C/CCCC(O)=O YIBNHAJFJUQSRA-YNNPMVKQSA-N 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
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- 239000000344 soap Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
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- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
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- 208000024891 symptom Diseases 0.000 description 1
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- 239000003826 tablet Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 231100000378 teratogenic Toxicity 0.000 description 1
- 230000003390 teratogenic effect Effects 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 229940117013 triethanolamine oleate Drugs 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 208000019553 vascular disease Diseases 0.000 description 1
- 229940124549 vasodilator Drugs 0.000 description 1
- 239000003071 vasodilator agent Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
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- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
- C07D307/935—Not further condensed cyclopenta [b] furans or hydrogenated cyclopenta [b] furans
- C07D307/937—Not further condensed cyclopenta [b] furans or hydrogenated cyclopenta [b] furans with hydrocarbon or substituted hydrocarbon radicals directly attached in position 2, e.g. prostacyclins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C405/00—Compounds containing a five-membered ring having two side-chains in ortho position to each other, and having oxygen atoms directly attached to the ring in ortho position to one of the side-chains, one side-chain containing, not directly attached to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having oxygen atoms attached in gamma-position to the ring, e.g. prostaglandins ; Analogues or derivatives thereof
Definitions
- Prostacyclin is a potent vasodilator and a potent inhibitor of platelet aggregation. These properties are opposite to those produced by thromboxane A 2 (TXA 2 ) which like PGI 2 is a major metabolite of the prostaglandin endoperoxides PGH 2 and PGG 2 .
- TXA 2 thromboxane A 2
- PGI 2 is a major metabolite of the prostaglandin endoperoxides
- prostacyclins in vivo prevent the attachment of platelet aggregates to blood vessel walls thereby inhibiting blood platelet aggregation while also lowering blood pressure.
- Prostacyclins as therapeutic agents suffer from the inherent disadvantage that they contain a labile enol ether moiety which causes instability.
- prostacyclins can be used both for their blood pressure lowering and platelet anti-aggregation effect. Therefore, a prostacyclin which is stable and which provides a separation between the anti-aggregation property and the blood pressure lowering effect is ideally suited for use as a therapeutic agent.
- R is hydrogen or lower alkyl
- R 2 is hydrogen, methyl or fluoro
- R 2 ' is fluoro, hydrogen, trifluoromethyl or methyl; and with the proviso that when R 2 ' is trifluoromethyl, R 2 is hydrogen or methyl
- the compounds of formulae I-A provide a separation of properties since they exhibit strong a blood platelet anti-aggregating affects without substantially reducing blood pressure. In addition, these compounds show a high degree of stability.
- the compounds of formulae I-A and I-B are prepared from compounds of the formula: ##STR2## wherein R 2 and R 2 ' are as above; R 3 and R 4 individually are hydrogen or when taken together with their attached oxygen atom form an ether or ester protecting group;
- lower alkyl includes both straight chain and branched chain alkyl groups having from 1 to 7 carbon atoms such as methyl and ethyl.
- lower alkanoic acids comprehends an alkanoic acid of 1 to 7 carbon atoms such as formic acid and acetic acid.
- halogen or “halo”, unless otherwise stated, comprehends fluorine, chlorine, bromine and iodine.
- Alkali metal includes all alkali metals such as lithium, sodium and potassium.
- all compounds having one or more asymmetric carbon atoms can be produced as racemic mixtures. These racemic mixtures which are obtained can be resolved at the appropriate steps in the process of this invention by methods well known in the art whereupon subsequent products may be obtained as the corresponding optically pure enantiomers.
- the claimed optically active enantiomer or racemates of formula I can be produced depending upon the optical form of the compound of formula II utilized as a starting material.
- a thickened taper line ( ) indicates a substituent which is in the beta-orientation (above the plane of the molecule)
- a dotted line ( ) indicates a substituent which is in the alpha-orientation (below the plane of the molecule)
- a wavy line ( ) indicates a substituent which is in either the alpha- or beta-orientation or mixtures of these isomers.
- aryl signifies mononuclear aromatic hydrocarbon groups such as phenyl, which can be unsubstituted or substituted in one or more positions with a lower alkylenedioxy, nitro, halo, a lower alkyl or a lower alkoxy substituent, and polynuclear aryl groups such as naphthyl, anthryl, phenanthryl, azulyl, etc., which can be unsubstituted or substituted with one or more of the aforementioned groups.
- the preferred aryl groups are the substituted and unsubstituted mononuclear aryl groups, particularly phenyl.
- ether protecting group removable by acid catalyzed cleavage designates any ether which, upon acid catalyzed cleavage yields the hydroxy group.
- a suitable ether protecting group is, for example, the tetrahydropyranyl ether, or 4-methoxy-tetrahydropyranyl ether.
- arylmethyl ethers such as benzyl, benzylhydryl, or trityl ethers or alpha-lower alkoxy lower alkyl ether, for example, methoxymethyl or tri(lower alkyl)silyl ethers such as trimethyl silyl ether; diphenyl-t-butyl silyl ether or dimethyl-tert-butyl silyl ethers.
- the preferred ether protecting groups which are removed by acid catalyzed cleavage are t-butyl and tetrahydropyranyl and the tri(lower alkyl and/or aryl)silyl ethers, particularly dimethyl-tert-butyl silyl ether and diphenyl-t-butyl silyl ether.
- Acid catalyzed cleavage is carried out by treatment with an organic or inorganic acid.
- the preferred inorganic acids are the mineral acids such as sulfuric acid, hydrohalic acid, etc.
- the preferred organic acids are lower alkanoic acids such as acetic acid, para-toluene sulfonic acid, etc.
- the acid catalyzed cleavage can be carried out in an aqueous medium or in an organic solvent medium. Where an organic acid or alcohol is utilized, the organic acid or alcohol can be the solvent medium. In the case of tetrahydropyranyl ethers, the cleavage is generally carried out in an aqueous medium. In carrying out this reaction, temperature and pressure are not critical and this reaction can be carried out at room temperature and atmosphere pressure.
- esters protecting group describes ester protecting groups where the hydroxy substituent is protected by esterification with an organic acid to form a hydrolizable ester.
- preferred esters which can be utilized to protect the hydroxy group are those esters formed by reacting the hydroxy group with a lower alkanoic acid containing from 1 to 7 carbon atoms present as acetic acid, propionic acid, butyric acid, as well as aroic acids such as benzoic acid and aryl lower alkanoic acids where aryl is defined as above and the lower alkanoic acid contains from 2 to 7 carbon atoms.
- Compound A (5Z,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-dihydroxy-prost-5-en-1-oic acid monosodium salt;
- Compound B (5Z,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-prost-5-en-1-oic acid monosodium salt;
- the IC 50 the dose at which the optical density of the samples decrease to a value which is fifty (50%) percent of the value of the control was determined by the method disclosed in Professor Born's article.
- the IC 50 values for the minimum dose were made from concentration response curve. These IC 50 's were determined in two separate tests using PRP from two separate donors.
- the results of the minimum dose of each of the test compounds which reduces fifty (50%) percent of the aggregation of the platelets produced by any one of AA, PAF, or collagen is set forth in the following Table:
- the compounds of formulae I-A and I-B because of their potent blood platelet aggregation inhibiting activity are effective as anti-thrombotic agents and in treating disorders due to blood clotting.
- the compounds of this invention possess the property of increasing the levels of cyclic adenosine monophosphate (AMP) produced in blood platelets.
- Cyclic AMP prevents aggregation of blood platelets. Through increasing cyclic AMP, the compounds of this invention prevent blood platelet aggregation. That the compounds of this invention increase cyclic AMP can be seen from the following test.
- human platelet rich plasma PRP was prepared by centrifugation of blood treated with 0.38% by weight sodium citrate at 180 ⁇ g (times gravity) for ten minutes.
- the PRP 50 ml containing approximately 2 ⁇ 10 7 platelets
- the reaction is incubated for two minutes at 22 C., with and without the test compound, in a Tris-HCl buffer for ten minutes pH 7.4 containing 5.5 mM HCl, 1 mM MgSO 4 , 5 mM Na 2 HPO 4 , 120 mM NaCl, and 5.5 mM glucose in a fluid volume of 250 ml.
- the reaction was terminated by placing the samples in boiling water for 3 minutes.
- the compounds of formulae I-A and I-B and their pharmaceutically acceptable salts because of their stability and their ability to inhibit blood platelet aggregation are effective in alleviating symptoms of periferal vascular diseases.
- the compounds of formulae I-A and I-B or their pharmaceutically acceptable salts can be used in a variety of pharmaceutical preparations.
- these compounds or their salts are administerable in the form of tablets, pills, powders, capsules, injectables, solutions, suppositories, emulsions, dispersions, and in other suitable forms.
- the pharmaceutical preparations which contain the compounds of formulae I-A and I-B or their pharmaceutically acceptable salts are conveniently formed by admixing them with a non-toxic pharmaceutical organic or inorganic carrier.
- Typical of pharmaceutically acceptable carriers are, for example, water, gelatin, lactose, starch, magnesium stearate, talc, vegetable oils, polyalkylene glycols, petroleum jelly and other conventionally employed pharmaceutically acceptable carriers.
- the pharmaceutical preparations may also contain non-toxic auxiliary substances such as emulsifying, preserving and wetting agents and the like, as for example, sorbitan monolaurate, triethanol amine oleate, polyoxyethylene sorbitan, dioctyl sodium sulfosuccinate and the like.
- the daily dose administered for the compounds will, of course, vary with the particular novel compound employed because of the very potency of the compounds, the chosen route of administration and the size of the recipient.
- the dosage administered is not subject to definite bounds but it will usually be in effective amounts of the pharmacologically function of the prostacyclin.
- Representative of a typical method for administering the prostacyclin compounds of formulae I-A and I-B or pharmaceutically acceptable salts thereof is by oral administration.
- the prostacyclins of formulae I-A and I-B or their salts can be administered at a dosage of 0.1 micrograms to 0.50 milligrams per day per kilogram of body weight.
- the compounds of formula I-A and I-B and salts thereof can be administered to the skin in preparations for topical administrations such as solutions, suspensions, ointments, creams, gels, micronized powders, aerosols and the like.
- the pharmaceutical preparations may be sterilized and/or may contain adjuvants such as preservatives, stabilizers, wetting agents, emulsifiers, salts for varying the osmotic pressure and/or buffers.
- the aforementioned compounds or their salts are preferably prepared as ointments, tinctures, creams, gels, solutions, lotions, sprays, suspensions, shampoos, hair soaps, perfumes and the like.
- any conventional composition utilized for application to the scalp or skin can be utilized in accordance with this invention.
- the composition containing the agents of this invention is in the form of gel, lotion and cream solutions.
- the pharmaceutical preparation for topical administration to the skin can be prepared by mixing the aforementioned active ingredient with non-toxic, therapeutically inert, solid or liquid carriers customarily used in such preparations. These preparations should contain at least about 0.0005 percent by weight, of the active ingredient based upon the total weight of the composition.
- the active ingredient is non-toxic, non-teratogenic and non-irritating it may be used in topical compositions in amounts significantly exceeding 10 percent i.e. up to 20% by weight. It is however preferred that these preparations contain about 0.01 to 10 percent by weight of the active ingredient based upon the total weight of the composition. It is also preferred to apply these preparations once or twice daily to the skin. These preparations can be applied according to the need of the patient.
- the active ingredient can be applied in an aqueous solution or an alcohol solution such as ethyl alcohol.
- additives such as preservatives, thickeners, perfumes, and the like conventional in the art of pharmaceutical compounding of topical preparations can be used.
- conventional antioxidants or mixtures of conventional antioxidants can be incorporated into the topical preparations containing the aforementioned active agent.
- the conventional antioxidants which can be utilized in these preparations are included N-methyl-a-tocopherolamine, tocopherols, butylated hydroxyanisole, butylatedhydroxytoluene, ethoxyquin and the like.
- Cream-base pharmaceutical formulations containing the active agent, used in accordance with this invention are composed of aqueous emulsions containing a fatty acid alcohol, semi-solid petroleum hydrocarbon, 1,2-ethyleneglycol and an emulsifying agent.
- Ointment formulations containing the active agent in accordance with this invention comprise admixtures of a semi-solid petroleum hydrocarbon with a solvent dispersion of the active material.
- Cream compositions containing the active ingredient for use in this invention preferably comprise emulsions formed from a water phase of a humectant, a viscosity sterilizer and water, an oil phase of fatty acid alcohol, a semisolid petroleum hydrocarbon and an emulsifying agent and a phase containing the active agent dispersed in an aqueous stabilizer-buffer solution.
- Stabilizers may be added to the topical preparation. Any conventional stabilizer can be utilized in accordance with this invention.
- fatty acid alcohol components function as a stabilizer.
- fatty acid alcohol components are derived from the reduction of a long-chain saturated fatty acid of at least 14 carbon atoms.
- conventional perfumes and lotions generally utilized in topical preparation for the hair can be utilized in accordance with this invention.
- conventional emulsifying agents can be utilized in the topical preparations of this invention.
- the preferred compound of formulae I-A and I-B are those compounds where the 7-fluoro substituent is in the beta configuration since these compounds are prepared easily in high yields.
- the compounds where the 7-fluoro substituted is in the alpha position are also preferred due to their enhanced stability.
- the 7-beta fluoro compounds the following are preferred: ##STR3## where R is hydrogen or lower alkyl When R is lower alkyl in the compound of formulae I-Ai and I-Aii, R is preferably methyl or ethyl.
- the compound of formula II is converted to a compound of the formula: ##STR4## wherein R 2 , R 2 ', R 3 and R 4 are as above; by hydrogenation utilizing conventional hydrogenation catalysts such as palladium, rhodium and platinum.
- conventional hydrogenation catalysts such as palladium, rhodium and platinum.
- this reaction can be carried out with R 3 and R 4 being hydrogen.
- one or both of the hydroxyl substituents on the compounds of formula II may be protected with either an ether or an ester protecting group prior to being subjected to hydrogenation to produce the compounds of formula III.
- R 3 and R 4 can be any conventional ether or ester protecting group such as the ether protecting groups removable by acid catalyzed cleavage or the ester groups removable by hydrolysis.
- the compound of formula III can be converted to the compound of formula III-B by reaction with a tri(lower alkyl and/or aryl)halosilane, preferably t-butyl-dimethyl chlorosilane. Any of the conditions conventional in reacting a hydroxy compound with a halosilane to form a siloxy derivative can be used in carrying out this reaction.
- R 3 and R 4 in the compound of formula III are a cleavable ether protecting group other than a tri(lower alkyl and/or aryl)silyl group, the protecting group can be cleaved by procedures well known in the art to produce a compound of the formula III where R 3 and R 4 are hydrogen.
- R 3 and R 4 from a hydrolyzable ester groups can be hydrolyzed by conventional means to form compounds of formula III where R 3 and R 4 are hydrogen. These latter compounds can be converted to the compound of formula III-B by reaction with a tri(lower alkyl and/or aryl)halosilane as described above.
- the compounds of formulae I-A and I-B are prepared from the compound of formula III-B via the following intermediates: ##STR6## wherein R 2 , R 2 ' and R 5 are as above; R 6 is lower alkyl and X is halogen; and R 7 is tri(lower alkyl and/or aryl)silyl.
- the compound of formula III-B is converted to the compound of formula V by first enolizing the compound of formula III-B and then treating the enolized form of the compound of formula III-B with a tri(alkyl and/or aryl)halosilane.
- Any conventional method of enolizing can be utilized to enolize the compound of formula III-B.
- the preferred methods is by treating the compound of formula III-B with a non-aqueous alkali metal base.
- the preferred base for use in this reaction is lithium diisopropyl amide or sodium hexamethyldisilazane.
- temperatures of -70° C. to 30° C. are generally preferred.
- this reaction is carried out in an inert organic solvent.
- Any conventional inert organic solvent which is a liquid at the aforementioned temperatures can be utilized.
- the preferred solvents are tetrahydrofuran.
- the enolate of the compound of formula III-B in the form of its alkali metal salt is converted to the compound of formula V by treating with a tri(alkyl and/or aryl)halosilane, preferably trimethylchlorosilane.
- this reaction is carried out at the same temperatures and in the same solvent utilized to form the enolate.
- the compound of formula V is converted to the compound of formula VI by treating the compound of formula V with a fluorinating agent.
- a fluorinating agent Any conventional fluorinating agent can be utilized in carrying out this reaction.
- the preferred fluorinating agents is xenon difluoride.
- this reaction is carried out in the presence of an inert organic solvent.
- Any conventional inert organic solvent can be utilized in carrying out this reaction.
- the preferred solvents are halogenated hydrocarbons such as methylene chloride, carbon tetrachloride, etc.
- temperature and pressure are not critical and this reaction can be carried out at room temperature and atmospheric pressure. While room temperature can be utilized, it is preferred to carry out this reaction at low temperatures, i.e. from -10° C. to +10° C.
- the compound of formula VI is produced as a mixture of the following compounds: ##STR7## wherein R 2 , R 2 ' and R 5 are as above.
- the compounds of formulae VI-A and VI-B can be separated by conventional methods such as chromatography.
- the compound of formula VI as a mixture of the compounds of formulae VI-A and VI-B can be utilized throughout the rest of the reactions or, if desired, separated at some later state in the reaction scheme to produce the compound of formula I-A or I-B having the desired fluoro orientation at the 7-position. If the compound of formula VI is separated into the compound of formulae VI-A and VI-B, the same configuration of the fluorine atom is carried out throughout the rest of the reactions to produce the compounds of formula IA or IB.
- the compound of formula VI-A is utilized in the rest of the reaction scheme to produce compounds of the formulae VIII through XVI wherein the 7-fluoro substituent in these formulae is in the beta position. If the compounds of I-A and I-B are desired wherein the fluoro substituent is in the 7-alpha position, then the compound of formula VI-B is utilized in the reaction scheme to produce the compounds of formulae VIII through XVI wherein the fluoro substituent shown in these formulae is in the alpha position.
- the compound of formula VI can be utilized without separating into the compounds of formulae VI-A and VI-B.
- the compounds of formulae I-A and I-B wherein the 7-fluoro substituent is in both the alpha and beta positions is produced via intermediates of the formulae VIII through XVI having the 7-fluoro group in both positions as shown.
- the compound of formula VI is converted to the compound of formula VIII by treating the compound of formula VI with a reducing agent.
- a reducing agent which will selectively reduce a lactone to a lactol
- Preferred reducing agents are the hydrides, particularly the aluminum hydrides such as alkali metal aluminum hydride, and the borohydrides such as alkali metal borohydrides, with diisobutyl aluminum hydride being particularly preferred.
- this reaction can be carried out utilizing di(branched chain lower alkyl)boranes such as bis(3-methyl-2-butyl)borane.
- temperature and pressure are not critical and the reaction can be carried out at room temperature and atmospheric pressure or at elevated or reduced temperatures and pressures.
- This reduction reaction can be carried out in the presence of an inert organic solvent.
- an inert organic solvent Any of the conventional inert organic solvents can be utilized in carrying out this reaction.
- the preferred solvents are dimethoxy ethylene glycol, and the ethers such as tetrahydrofuran, diethyl ether and dioxane.
- the compound of formula IX is obtained from the compound of formula VIII by reaction the compound of formula VIII with phosphonium salts of the formula: ##STR8## wherein R 15 , R 15 ', R 15 " is aryl or di(lower alkyl)amino; and Y is halogen
- the compound of formula IX can be converted to a compound of the formula X by esterification with diazomethane or a reactive derivative of a lower alkanol such as a lower alkyl halide. Any conventional conditions utilizing in these esterifying reactions can be utilized to form the compound of formula X from the compound of formula IX.
- the compound of formula X is converted to the compound of formula XI by treating the compound of formula X with a halogenating agent.
- a halogenating agent include N-halosuccinimides, particularly N-iodosuccinimide.
- this reaction is carried out in the presence of a polar solvent such as acetonitrile and halogenated hydrocarbons such as methylene chloride, ethylene chloride, etc.
- a polar solvent such as acetonitrile and halogenated hydrocarbons such as methylene chloride, ethylene chloride, etc.
- any conventional polar organic solvent can be utilized.
- temperature of from 0° C. to 35° C. can be utilized.
- the compound of formula XI is converted to the compound of formula XII by ether cleavage. Any conventional method of ether cleavage described hereinbefore can be utilized to carry out this reaction.
- the compound of formula XII is treated with a dehydrohalogenating agent to produce the compounds of formulae XIII and XIV in admixture.
- a dehydrohalogenating agent can be utilized.
- the preferred dehydrohalogenating agents are the diazabicycloalkanes or alkanes such as 1,8-diazabicyclo[5.4.0]undec-7-ene and 1,4-diazabicyclo[2.2.2]octane.
- any other conventional organic base utilized for dehydrohalogenation can be utilized in carrying out this reaction.
- This reaction produces the compounds of formula XIII and the compounds of formula XIV in admixture.
- the compounds of formula XIII can be separated from the compounds of formula XIV by any conventional separation procedure such as chromatography.
- the compound of formula XIII can be converted to the compound of formula XV and the compound of formula XIV is converted to the compound of formula XVI by hydrolysis.
- Any conventional method of ester hydrolysis can be utilized in carrying out these reactions.
- the preferred method of ester hydrolysis is either treating the compound of formula XIII or the compound of formula XIV with a alkali metal hydroxide.
- the preferred alkali metal hydroxides for use in this reaction are sodium and potassium hydroxides.
- any pharmaceutically acceptable basic salts of the compound of formula I-A and I-B where R is hydrogen can be utilized.
- the alkali metal salts such as lithium, sodium, and potassium, with sodium being especially preferred.
- Other salts which are also preferred are the alkaline earth metal salts such as calcium and magnesium, amine salts such as the lower alkyl amines, e.g. ethylamine and the hydroxy-substituted lower alkyl amine salts and tris(hydroxymethyl)aminomethane.
- ammonium salts are also preferred.
- the other salts are dibenzylamine, monoalkylamines or dialkylamine and salts with amino acids (i.e. salts with arginine and glycine).
- the ethyl acetate solution was washed with water; the water layer saturated with NaCl and extracted with additional ethyl acetate.
- the ethyl acetate solutions were combined and dried (MgSO 4 ).
- the solvent was then removed under reduced pressure and the residue chromatographed on 400 g of silica gel (5% by volume ethyl acetate/95% by volume hexane - ⁇ ethyl acetate) to give 11 g of the diol, i.e. 3aR-[3a alpha,4alpha(3S*),5beta,6a alpha]]-5-hydroxy-4-(3-hydroxyoctyl)-2H-cyclopenta[b]furan-2-one.
- This compound was then dissolved at 0° C. in 50 ml of dry CH 2 Cl 2 containing 5.26 g of KHCO 3 , followed by the slow addition of 5.0 g of xenon difluoride. The mixture was then stirred for an additional 0.5 hr at 0° C. and then poured into 500 ml of ice water followed by extraction with CH 2 Cl 2 . The organic layer was separated, dried, and the solvent removed under reduced pressure.
- the solution was allowed to stir an additional twenty minutes at -70° C. after which time 20 ml of a saturated NH 4 Cl solution was added slowly. The mixture was then warmed to 15° C. diluted with 200 ml of ethyl acetate and washed with a saturated NaCl solution. The washings were extracted with ethyl acetate. The ethyl acetate solutions were combined and dried (MgSO 4 ).
- the mixture was then partitioned between 500 ml of ether and 300 ml of H 2 O at 0° C. and then treated with 1N HCl to pH 3. The layers were separated and the water washed with a saturated NaCl solution and dried (MgSO 4 ).
- the ether was then removed under reduced pressure to give 15 g of a light yellow oil containing (5Z,7R,9alpha,11alpha,15S)-7-fluoro-11,13-bis-[[(1,1-dimethylethyl)dimethylsilyl]oxy]prost-5-en-1-oic acid.
- the crude acid was then taken up in 50 ml of dry CH 2 Cl 2 and treated with an ethereal solution of diazomethane. The excess diazomethane was blown off with a stream of argon. The residue was taken up in ether, dried (MgSO 4 ), and the solvent removed under reduced pressure.
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Abstract
7-fluoro-16-substituted 15-hydroxy PGI2 compounds which have saturated bond of the 13 position and which are useful as blood platelet anti-aggregating agents.
Description
This application is a divisional of U.S. application, Ser. No. 747,740, filed June 24, 1985--Holland et al, now U.S. Pat. No. 4,634,782, issued Jan. 6, 1987.
Prostacyclin (PGI2) is a potent vasodilator and a potent inhibitor of platelet aggregation. These properties are opposite to those produced by thromboxane A2 (TXA2) which like PGI2 is a major metabolite of the prostaglandin endoperoxides PGH2 and PGG2. Generally, prostacyclins in vivo prevent the attachment of platelet aggregates to blood vessel walls thereby inhibiting blood platelet aggregation while also lowering blood pressure.
7-halo PGI2 derivatives have been described and found useful for inhibiting blood platelet aggregation while lowering blood pressure. See for example British Patent Application No. 2,094,310--Holland, Maag and Rosen published Sept. 15, 1982; British Patent Application No. 2,088,856--Szekely et al. published June 19, 1982 and U.S. Pat. No. 4,472,428--Toru et al. issued Sept. 18, 1984.
Prostacyclins as therapeutic agents suffer from the inherent disadvantage that they contain a labile enol ether moiety which causes instability. In addition prostacyclins can be used both for their blood pressure lowering and platelet anti-aggregation effect. Therefore, a prostacyclin which is stable and which provides a separation between the anti-aggregation property and the blood pressure lowering effect is ideally suited for use as a therapeutic agent.
In accordance with this invention, compounds of the formula ##STR1## wherein R is hydrogen or lower alkyl; R2 is hydrogen, methyl or fluoro; and R2 ' is fluoro, hydrogen, trifluoromethyl or methyl; and with the proviso that when R2 ' is trifluoromethyl, R2 is hydrogen or methyl
and salts thereof as well as optical antipodes and racemates thereof are useful as a blood platelet anti-aggregating agents. In particular, the compounds of formulae I-A provide a separation of properties since they exhibit strong a blood platelet anti-aggregating affects without substantially reducing blood pressure. In addition, these compounds show a high degree of stability.
The compounds of formulae I-A and I-B are prepared from compounds of the formula: ##STR2## wherein R2 and R2 ' are as above; R3 and R4 individually are hydrogen or when taken together with their attached oxygen atom form an ether or ester protecting group;
or optical antipodes or racemates thereof.
As used throughout this application, the term "lower alkyl" includes both straight chain and branched chain alkyl groups having from 1 to 7 carbon atoms such as methyl and ethyl. As also used herein, the term "lower alkanoic acids" comprehends an alkanoic acid of 1 to 7 carbon atoms such as formic acid and acetic acid. As further used herein, the the term "halogen" or "halo", unless otherwise stated, comprehends fluorine, chlorine, bromine and iodine. Alkali metal includes all alkali metals such as lithium, sodium and potassium.
In the process of this invention, all compounds having one or more asymmetric carbon atoms can be produced as racemic mixtures. These racemic mixtures which are obtained can be resolved at the appropriate steps in the process of this invention by methods well known in the art whereupon subsequent products may be obtained as the corresponding optically pure enantiomers. On the other hand, the claimed optically active enantiomer or racemates of formula I can be produced depending upon the optical form of the compound of formula II utilized as a starting material.
In the pictorial representation of the compounds given throughout this application, a thickened taper line ( ) indicates a substituent which is in the beta-orientation (above the plane of the molecule), a dotted line ( ) indicates a substituent which is in the alpha-orientation (below the plane of the molecule) and a wavy line ( ) indicates a substituent which is in either the alpha- or beta-orientation or mixtures of these isomers. It is to be understood that the pictorial representations of the compounds given throughout the specification are set forth for convenience and are to be construed as inclusive of other forms including enantiomers and racemates and are not to be construed as limited to the particular form shown.
As also used herein, the term "aryl" signifies mononuclear aromatic hydrocarbon groups such as phenyl, which can be unsubstituted or substituted in one or more positions with a lower alkylenedioxy, nitro, halo, a lower alkyl or a lower alkoxy substituent, and polynuclear aryl groups such as naphthyl, anthryl, phenanthryl, azulyl, etc., which can be unsubstituted or substituted with one or more of the aforementioned groups. The preferred aryl groups are the substituted and unsubstituted mononuclear aryl groups, particularly phenyl.
The term "ether protecting group removable by acid catalyzed cleavage" designates any ether which, upon acid catalyzed cleavage yields the hydroxy group. A suitable ether protecting group is, for example, the tetrahydropyranyl ether, or 4-methoxy-tetrahydropyranyl ether. Others are arylmethyl ethers such as benzyl, benzylhydryl, or trityl ethers or alpha-lower alkoxy lower alkyl ether, for example, methoxymethyl or tri(lower alkyl)silyl ethers such as trimethyl silyl ether; diphenyl-t-butyl silyl ether or dimethyl-tert-butyl silyl ethers. The preferred ether protecting groups which are removed by acid catalyzed cleavage are t-butyl and tetrahydropyranyl and the tri(lower alkyl and/or aryl)silyl ethers, particularly dimethyl-tert-butyl silyl ether and diphenyl-t-butyl silyl ether. Acid catalyzed cleavage is carried out by treatment with an organic or inorganic acid. Among the preferred inorganic acids are the mineral acids such as sulfuric acid, hydrohalic acid, etc. Among the preferred organic acids are lower alkanoic acids such as acetic acid, para-toluene sulfonic acid, etc. The acid catalyzed cleavage can be carried out in an aqueous medium or in an organic solvent medium. Where an organic acid or alcohol is utilized, the organic acid or alcohol can be the solvent medium. In the case of tetrahydropyranyl ethers, the cleavage is generally carried out in an aqueous medium. In carrying out this reaction, temperature and pressure are not critical and this reaction can be carried out at room temperature and atmosphere pressure.
The term "ester protecting group" describes ester protecting groups where the hydroxy substituent is protected by esterification with an organic acid to form a hydrolizable ester. Among the preferred esters which can be utilized to protect the hydroxy group are those esters formed by reacting the hydroxy group with a lower alkanoic acid containing from 1 to 7 carbon atoms present as acetic acid, propionic acid, butyric acid, as well as aroic acids such as benzoic acid and aryl lower alkanoic acids where aryl is defined as above and the lower alkanoic acid contains from 2 to 7 carbon atoms.
That the 7-fluoro prostacyclins are potent blood platelet anti-aggregating agents can be seen when the following compounds
Compound A=(5Z,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-dihydroxy-prost-5-en-1-oic acid monosodium salt; and
Compound B=(5Z,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-prost-5-en-1-oic acid monosodium salt;
were tested against PGI2 for their blood platelet anti-aggregation properties by the standard test described by Professor Born in Nature, 194 927, (1962).
In this test, the ability of the above compounds to inhibit aggregation of blood platelets in 0.45 ml of human platelet rich plasma (PRP) was measured. Aggregation was induced by the addition of any one of arachidonic acid (AA), platelet activating factor (PAF) or collagen. PAF and its synthesis is disclosed by Hirth and Barner in Helv. Chim. Acta. Vol. 65; Fasc. 3, page 1059 (1982) [Compound 1-a on page 1061]. By titration of AA, collagen and PAF at various concentrations in 0.45 ml samples of PRP, the minimum amount of AA, collagen and PAF which produces maximum blood platelet aggregation in a given sample of human platelet rich plasma (PRP) was determined. This minimum amount was used when the compounds set forth above were tested for their ability to inhibit blood platelet aggregation in samples of PRP as described below.
In carrying out the tests, various concentrations of the test compound were added to separate samples of human platelet rich plasma (PRP). To each of these samples of PRP containing a specific concentration of one of the above test compounds, there was added the minimum amount of AA, PAF, or collagen calculated above. The controls are samples of PRP containing no test compound but only the minimum amount of AA, PAF, or collagen determined above. The percent aggregation of the various samples was determined by measuring the optical density of the samples and comparing them with the optical density of the controls. This determination was made two minutes after the maximum first phase response of PAF, AA or collagen. This determination was made with freshly prepared samples of test compounds. A second determination was made in the same manner with samples of PRP two hours after the addition of AA, PAF or collagen. The IC50, the dose at which the optical density of the samples decrease to a value which is fifty (50%) percent of the value of the control was determined by the method disclosed in Professor Born's article. The IC50 values for the minimum dose were made from concentration response curve. These IC50 's were determined in two separate tests using PRP from two separate donors. The results of the minimum dose of each of the test compounds which reduces fifty (50%) percent of the aggregation of the platelets produced by any one of AA, PAF, or collagen is set forth in the following Table:
TABLE 1 ______________________________________ Aggregation IC.sub.50 (nm) Compound AA PAF Collagen ______________________________________ PGI.sub.2 0.45 0.15 2 Compound A 23 15 -- Compound B 20 6 6 ______________________________________
The compounds of formulae I-A and I-B because of their potent blood platelet aggregation inhibiting activity are effective as anti-thrombotic agents and in treating disorders due to blood clotting.
The compounds of this invention possess the property of increasing the levels of cyclic adenosine monophosphate (AMP) produced in blood platelets. Cyclic AMP prevents aggregation of blood platelets. Through increasing cyclic AMP, the compounds of this invention prevent blood platelet aggregation. That the compounds of this invention increase cyclic AMP can be seen from the following test.
In this test, human platelet rich plasma (PRP) was prepared by centrifugation of blood treated with 0.38% by weight sodium citrate at 180×g (times gravity) for ten minutes. The PRP (50 ml containing approximately 2×107 platelets) is incubated for two minutes at 22 C., with and without the test compound, in a Tris-HCl buffer for ten minutes pH 7.4 containing 5.5 mM HCl, 1 mM MgSO4, 5 mM Na2 HPO4, 120 mM NaCl, and 5.5 mM glucose in a fluid volume of 250 ml. The reaction was terminated by placing the samples in boiling water for 3 minutes. The boiled extract was assayed for cyclic AMP by the protein binding method of Brown et al. (Biochemical Journal 121:561-562, 1971). The activity of this test compound at 0.1 mM is measured as the percent increase in cyclic AMP production compared to base 1 (vehicle alone) production. The results are given below:
______________________________________ Cyclic AMP Production o/o stimulative of Compound Basal at 0.1 mM ______________________________________ PGI.sub.2 3721 Compound A 998 Compound B 1353 ______________________________________
The compounds of formulae I-A and I-B and their pharmaceutically acceptable salts because of their stability and their ability to inhibit blood platelet aggregation are effective in alleviating symptoms of periferal vascular diseases.
The compounds of formulae I-A and I-B or their pharmaceutically acceptable salts can be used in a variety of pharmaceutical preparations. In these preparations, these compounds or their salts are administerable in the form of tablets, pills, powders, capsules, injectables, solutions, suppositories, emulsions, dispersions, and in other suitable forms. The pharmaceutical preparations which contain the compounds of formulae I-A and I-B or their pharmaceutically acceptable salts are conveniently formed by admixing them with a non-toxic pharmaceutical organic or inorganic carrier. Typical of pharmaceutically acceptable carriers are, for example, water, gelatin, lactose, starch, magnesium stearate, talc, vegetable oils, polyalkylene glycols, petroleum jelly and other conventionally employed pharmaceutically acceptable carriers. The pharmaceutical preparations may also contain non-toxic auxiliary substances such as emulsifying, preserving and wetting agents and the like, as for example, sorbitan monolaurate, triethanol amine oleate, polyoxyethylene sorbitan, dioctyl sodium sulfosuccinate and the like.
The daily dose administered for the compounds will, of course, vary with the particular novel compound employed because of the very potency of the compounds, the chosen route of administration and the size of the recipient. The dosage administered is not subject to definite bounds but it will usually be in effective amounts of the pharmacologically function of the prostacyclin. Representative of a typical method for administering the prostacyclin compounds of formulae I-A and I-B or pharmaceutically acceptable salts thereof is by oral administration. By this route, the prostacyclins of formulae I-A and I-B or their salts can be administered at a dosage of 0.1 micrograms to 0.50 milligrams per day per kilogram of body weight.
The compounds of formula I-A and I-B and salts thereof and can be administered to the skin in preparations for topical administrations such as solutions, suspensions, ointments, creams, gels, micronized powders, aerosols and the like. The pharmaceutical preparations may be sterilized and/or may contain adjuvants such as preservatives, stabilizers, wetting agents, emulsifiers, salts for varying the osmotic pressure and/or buffers.
For topical administration to the skin the aforementioned compounds or their salts are preferably prepared as ointments, tinctures, creams, gels, solutions, lotions, sprays, suspensions, shampoos, hair soaps, perfumes and the like. In fact, any conventional composition utilized for application to the scalp or skin can be utilized in accordance with this invention. Among the preferred methods of applying the composition containing the agents of this invention is in the form of gel, lotion and cream solutions. The pharmaceutical preparation for topical administration to the skin can be prepared by mixing the aforementioned active ingredient with non-toxic, therapeutically inert, solid or liquid carriers customarily used in such preparations. These preparations should contain at least about 0.0005 percent by weight, of the active ingredient based upon the total weight of the composition. Since the active ingredient, the compound of formula I, is non-toxic, non-teratogenic and non-irritating it may be used in topical compositions in amounts significantly exceeding 10 percent i.e. up to 20% by weight. It is however preferred that these preparations contain about 0.01 to 10 percent by weight of the active ingredient based upon the total weight of the composition. It is also preferred to apply these preparations once or twice daily to the skin. These preparations can be applied according to the need of the patient. In carrying out this invention, the active ingredient can be applied in an aqueous solution or an alcohol solution such as ethyl alcohol.
In preparing the topical preparations described above additives such as preservatives, thickeners, perfumes, and the like conventional in the art of pharmaceutical compounding of topical preparations can be used. In addition, conventional antioxidants or mixtures of conventional antioxidants can be incorporated into the topical preparations containing the aforementioned active agent. Among the conventional antioxidants which can be utilized in these preparations are included N-methyl-a-tocopherolamine, tocopherols, butylated hydroxyanisole, butylatedhydroxytoluene, ethoxyquin and the like. Cream-base pharmaceutical formulations containing the active agent, used in accordance with this invention, are composed of aqueous emulsions containing a fatty acid alcohol, semi-solid petroleum hydrocarbon, 1,2-ethyleneglycol and an emulsifying agent.
Ointment formulations containing the active agent in accordance with this invention comprise admixtures of a semi-solid petroleum hydrocarbon with a solvent dispersion of the active material. Cream compositions containing the active ingredient for use in this invention preferably comprise emulsions formed from a water phase of a humectant, a viscosity sterilizer and water, an oil phase of fatty acid alcohol, a semisolid petroleum hydrocarbon and an emulsifying agent and a phase containing the active agent dispersed in an aqueous stabilizer-buffer solution. Stabilizers may be added to the topical preparation. Any conventional stabilizer can be utilized in accordance with this invention. In the oil phase, fatty acid alcohol components function as a stabilizer. These fatty acid alcohol components are derived from the reduction of a long-chain saturated fatty acid of at least 14 carbon atoms. Also, conventional perfumes and lotions generally utilized in topical preparation for the hair can be utilized in accordance with this invention. Furthermore, if desired, conventional emulsifying agents can be utilized in the topical preparations of this invention.
Among the preferred compound of formulae I-A and I-B are those compounds where the 7-fluoro substituent is in the beta configuration since these compounds are prepared easily in high yields. However, the compounds where the 7-fluoro substituted is in the alpha position are also preferred due to their enhanced stability. Among the 7-beta fluoro compounds, the following are preferred: ##STR3## where R is hydrogen or lower alkyl When R is lower alkyl in the compound of formulae I-Ai and I-Aii, R is preferably methyl or ethyl.
In preparing the compounds of this invention, the compound of formula II is converted to a compound of the formula: ##STR4## wherein R2, R2 ', R3 and R4 are as above; by hydrogenation utilizing conventional hydrogenation catalysts such as palladium, rhodium and platinum. In carrying out this reaction any of the conditions coventionally used in catalytic hydrogenation can be used. If desired, this reaction can be carried out with R3 and R4 being hydrogen. On the other hand, one or both of the hydroxyl substituents on the compounds of formula II may be protected with either an ether or an ester protecting group prior to being subjected to hydrogenation to produce the compounds of formula III. In the compound of formulae II and III, R3 and R4 can be any conventional ether or ester protecting group such as the ether protecting groups removable by acid catalyzed cleavage or the ester groups removable by hydrolysis.
In the next step in the production of the compounds of formula I-A and I-B, the compounds of formula III where R3 and R4 are other than a tri(lower alkyl and/or aryl)silyl protecting group are converted to compounds of the formula ##STR5## wherein R2 and R2 ' are as above; and R5 is tri(lower alkyl and/or aryl)silyl;
Where R3 and R4 in the compound of III are hydrogen, the compound of formula III can be converted to the compound of formula III-B by reaction with a tri(lower alkyl and/or aryl)halosilane, preferably t-butyl-dimethyl chlorosilane. Any of the conditions conventional in reacting a hydroxy compound with a halosilane to form a siloxy derivative can be used in carrying out this reaction. Where R3 and R4 in the compound of formula III are a cleavable ether protecting group other than a tri(lower alkyl and/or aryl)silyl group, the protecting group can be cleaved by procedures well known in the art to produce a compound of the formula III where R3 and R4 are hydrogen. On the other hand, where R3 and R4 from a hydrolyzable ester groups, these groups can be hydrolyzed by conventional means to form compounds of formula III where R3 and R4 are hydrogen. These latter compounds can be converted to the compound of formula III-B by reaction with a tri(lower alkyl and/or aryl)halosilane as described above.
The compounds of formulae I-A and I-B are prepared from the compound of formula III-B via the following intermediates: ##STR6## wherein R2, R2 ' and R5 are as above; R6 is lower alkyl and X is halogen; and R7 is tri(lower alkyl and/or aryl)silyl.
The compound of formula III-B is converted to the compound of formula V by first enolizing the compound of formula III-B and then treating the enolized form of the compound of formula III-B with a tri(alkyl and/or aryl)halosilane. Any conventional method of enolizing can be utilized to enolize the compound of formula III-B. Among the preferred methods is by treating the compound of formula III-B with a non-aqueous alkali metal base. The preferred base for use in this reaction is lithium diisopropyl amide or sodium hexamethyldisilazane. In carrying out the reaction utilizing the non-aqueous alkali metal base, temperatures of -70° C. to 30° C. are generally preferred. Generally, this reaction is carried out in an inert organic solvent. Any conventional inert organic solvent which is a liquid at the aforementioned temperatures can be utilized. Among the preferred solvents are tetrahydrofuran. The enolate of the compound of formula III-B in the form of its alkali metal salt is converted to the compound of formula V by treating with a tri(alkyl and/or aryl)halosilane, preferably trimethylchlorosilane. Generally, this reaction is carried out at the same temperatures and in the same solvent utilized to form the enolate.
The compound of formula V is converted to the compound of formula VI by treating the compound of formula V with a fluorinating agent. Any conventional fluorinating agent can be utilized in carrying out this reaction. Among the preferred fluorinating agents is xenon difluoride. Generally, this reaction is carried out in the presence of an inert organic solvent. Any conventional inert organic solvent can be utilized in carrying out this reaction. Among the preferred solvents are halogenated hydrocarbons such as methylene chloride, carbon tetrachloride, etc. In carrying out this reaction, temperature and pressure are not critical and this reaction can be carried out at room temperature and atmospheric pressure. While room temperature can be utilized, it is preferred to carry out this reaction at low temperatures, i.e. from -10° C. to +10° C.
In converting the compound of formula V to the compound of formula VI, the compound of formula VI is produced as a mixture of the following compounds: ##STR7## wherein R2, R2 ' and R5 are as above.
The compounds of formulae VI-A and VI-B can be separated by conventional methods such as chromatography. On the other hand, the compound of formula VI as a mixture of the compounds of formulae VI-A and VI-B can be utilized throughout the rest of the reactions or, if desired, separated at some later state in the reaction scheme to produce the compound of formula I-A or I-B having the desired fluoro orientation at the 7-position. If the compound of formula VI is separated into the compound of formulae VI-A and VI-B, the same configuration of the fluorine atom is carried out throughout the rest of the reactions to produce the compounds of formula IA or IB. Therefore, in producing the compounds of formulae I-A or I-B wherein the fluorine atom is at the 7-beta position, the compound of formula VI-A is utilized in the rest of the reaction scheme to produce compounds of the formulae VIII through XVI wherein the 7-fluoro substituent in these formulae is in the beta position. If the compounds of I-A and I-B are desired wherein the fluoro substituent is in the 7-alpha position, then the compound of formula VI-B is utilized in the reaction scheme to produce the compounds of formulae VIII through XVI wherein the fluoro substituent shown in these formulae is in the alpha position.
On the other hand, the compound of formula VI can be utilized without separating into the compounds of formulae VI-A and VI-B. In this manner, the compounds of formulae I-A and I-B wherein the 7-fluoro substituent is in both the alpha and beta positions is produced via intermediates of the formulae VIII through XVI having the 7-fluoro group in both positions as shown.
The compound of formula VI is converted to the compound of formula VIII by treating the compound of formula VI with a reducing agent. In carrying out this reaction, any conventional reducing agent which will selectively reduce a lactone to a lactol can be utilized. Preferred reducing agents are the hydrides, particularly the aluminum hydrides such as alkali metal aluminum hydride, and the borohydrides such as alkali metal borohydrides, with diisobutyl aluminum hydride being particularly preferred. Also, this reaction can be carried out utilizing di(branched chain lower alkyl)boranes such as bis(3-methyl-2-butyl)borane. In carrying out this reaction, temperature and pressure are not critical and the reaction can be carried out at room temperature and atmospheric pressure or at elevated or reduced temperatures and pressures. Generally, it is preferred to carry out this reaction at a temperature of from -80° C. to room temperature. This reduction reaction can be carried out in the presence of an inert organic solvent. Any of the conventional inert organic solvents can be utilized in carrying out this reaction. Among the preferred solvents are dimethoxy ethylene glycol, and the ethers such as tetrahydrofuran, diethyl ether and dioxane.
The compound of formula IX is obtained from the compound of formula VIII by reaction the compound of formula VIII with phosphonium salts of the formula: ##STR8## wherein R15, R15 ', R15 " is aryl or di(lower alkyl)amino; and Y is halogen
via a conventional Wittig type reaction. Any of the conventional conditions in Wittig reactions can be utilized in carrying out this reaction.
The compound of formula IX can be converted to a compound of the formula X by esterification with diazomethane or a reactive derivative of a lower alkanol such as a lower alkyl halide. Any conventional conditions utilizing in these esterifying reactions can be utilized to form the compound of formula X from the compound of formula IX.
The compound of formula X is converted to the compound of formula XI by treating the compound of formula X with a halogenating agent. Among the preferred halogenating agents are included N-halosuccinimides, particularly N-iodosuccinimide. Generally, this reaction is carried out in the presence of a polar solvent such as acetonitrile and halogenated hydrocarbons such as methylene chloride, ethylene chloride, etc. In fact, any conventional polar organic solvent can be utilized. In carrying out this reaction, temperature of from 0° C. to 35° C. can be utilized. Generally, it is preferred to carry out this reaction at room temperature.
The compound of formula XI is converted to the compound of formula XII by ether cleavage. Any conventional method of ether cleavage described hereinbefore can be utilized to carry out this reaction.
In the next step, the compound of formula XII is treated with a dehydrohalogenating agent to produce the compounds of formulae XIII and XIV in admixture. In carrying out this reaction, any conventional dehydrohalogenating agent can be utilized. Among the preferred dehydrohalogenating agents are the diazabicycloalkanes or alkanes such as 1,8-diazabicyclo[5.4.0]undec-7-ene and 1,4-diazabicyclo[2.2.2]octane. Furthermore, any other conventional organic base utilized for dehydrohalogenation can be utilized in carrying out this reaction. This reaction produces the compounds of formula XIII and the compounds of formula XIV in admixture. The compounds of formula XIII can be separated from the compounds of formula XIV by any conventional separation procedure such as chromatography.
The compound of formula XIII can be converted to the compound of formula XV and the compound of formula XIV is converted to the compound of formula XVI by hydrolysis. Any conventional method of ester hydrolysis can be utilized in carrying out these reactions. Among the preferred method of ester hydrolysis is either treating the compound of formula XIII or the compound of formula XIV with a alkali metal hydroxide. Among the preferred alkali metal hydroxides for use in this reaction are sodium and potassium hydroxides.
In the practice of this invention, any pharmaceutically acceptable basic salts of the compound of formula I-A and I-B where R is hydrogen can be utilized. Among the preferred pharmaceutically acceptable basic salts are included the alkali metal salts such as lithium, sodium, and potassium, with sodium being especially preferred. Other salts which are also preferred are the alkaline earth metal salts such as calcium and magnesium, amine salts such as the lower alkyl amines, e.g. ethylamine and the hydroxy-substituted lower alkyl amine salts and tris(hydroxymethyl)aminomethane. Also preferred are the ammonium salts. Among the other salts are dibenzylamine, monoalkylamines or dialkylamine and salts with amino acids (i.e. salts with arginine and glycine).
The following Examples are illustrative but not limitative of the invention. In the Examples, the ether utilized was diethyl ether. All temperatures are in degrees Centigrade. Celite is diatomaceous earth and DMF is dimethyl formamide.
To 2 g of platinum in 100 ml of ethyl acetate was added a solution of 19.8 g of (0.053 mol) of [3aR-[3a alpha,4alpha(1E,3S*),5beta,6a alpha]]-5-(benzoyloxy)hexahydro-4-(3-hydroxy-1-octenyl)-2H-cyclopenta[b]furan-2-one in 100 ml of ethyl acetate. The solution was then hydrogenated until the theoretical uptake of hydrogen was complete (ca. 2h) and then filtered through a bed of Celite. The solvent was then removed under reduced pressure to give 19.9 g of [3aR-[3a alpha,4alpha(3S*),5beta,6a alpha)]-5-(benzoyloxy)hexahydro-4-(3-hydroxyoctyl)-2H-cyclopenta[b]furan-2-one as colorless oil (100% yield) [a]D 25 -72.03 (CHCl3, C=0.794).
Anal. Calcd for C22 H30 O5 : C, 70.56, H, 8.80. Found: C, 70.51; H, 7.97.
To 1.1 g of platinum in 50 ml of ethyl acetate was added a solution of 11 g of (0.028 mol) of [3aR-[3a alpha,4alpha(1E,3R*,4S*),5beta,6a alpha]]-5-(benzoyloxy)-4-(4-fluoro-3-hydroxy-1-octenyl)hexahydro-2H-cyclopenta[b]furan-2-one in 110 ml of ethyl acetate. The mixture was then hydrogenated until the theoretical uptake of hydrogen was complete and then filtered through a bed of Celite. The solvent was then removed under reduced pressure and the residue chromatographed over 250 g of silica gel (toluene -∝ 30% by volume ethyl acetate/70% by volume toluene) to afford 10.7 g of [3aR-[3a alpha,4alpha(3R*,4S*),5beta,6a alpha)]-5-(benzoyloxy)-4-(4-fluoro-3-hydroxyoctyl)hexahydro-2H-cyclopenta[b]furan-2-one (94% yield) as a colorless oil.
Anal. Calcd for C22 H29 FO5 : C, 67.33; H, 7.45. Found: C, 66.80; H, 7.51.
To a solution of 20.5 g (0.055 mol) of [3aR-[3a alpha,4alpha-(3S*),5beta,6a alpha]]-5-(benzoyloxy)hexahydro-4-(3-hydroxyoctyl)-2H-cyclopenta-[b]furan-2-one dissolved in 200 ml of methanol was added 14.35 g of Na2 CO3. After 4 hr an additional 14.4 g of Na2 CO3, was added and then again 3 hr later. The mixture was then filtered and the Na2 CO3, washed with dry methanol. The methanol was removed under reduced pressure and the residue dissolved in ethyl acetate. The ethyl acetate solution was washed with water; the water layer saturated with NaCl and extracted with additional ethyl acetate. The ethyl acetate solutions were combined and dried (MgSO4). The solvent was then removed under reduced pressure and the residue chromatographed on 400 g of silica gel (5% by volume ethyl acetate/95% by volume hexane -∝ ethyl acetate) to give 11 g of the diol, i.e. 3aR-[3a alpha,4alpha(3S*),5beta,6a alpha]]-5-hydroxy-4-(3-hydroxyoctyl)-2H-cyclopenta[b]furan-2-one.
To 10.2 g of the diol dissolved in 150 ml of DMF was added 13.1 g of imidazole followed by 23.4 g of t-butyldimethylchlorosilane and the reaction mixture stirred for 18 hr. The mixture was then added to 500 ml of 0.5N NH4 Cl solution and the mixture extracted with 3×500 ml of ether. The combined ether extracts were washed with a saturated NaHCO3 solution followed by a saturated NaCl solution. The ether solution was then dried (MgSO4), the ether removed under reduced pressure and the residue chromatographed on 500 g of silica gel (10% by volume ether/90% by volume petroleum ether -∝ 20% by volume ether/80% by volume petroleum ether) to give 13.6 g of [3aR-[3a alpha,4alpha(3S*),5beta,6a alpha]]hexahydro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]octyl]-2H-cyclopenta[b]furan-2-one as a colorless oil.
Anal. Calcd for C27 H54 O4 Si2 : C, 65.00; H, 10.91. Found: C, 64.84; H, 11.03.
To a solution of 10.3 g (0.026 mol) of [3aR-[3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]-hexahydro-5-(benzoyloxy)-4-(4-fluoro-3-hydroxyoctyl)2H-cyclopenta[b]furan-2-one dissolved in 200 ml of CH3 OH was added 7 g of Na2 CO3. After several hours an additional 5 g of Na2 CO3 was added and the mixture allowed to stir overnight. The mixture was filtered and the solvent removed under reduced pressure. The residue was dissolved in CH2 Cl2, dried (MgSO4), and the solvent removed under reduced pressure. The resulting solid was then triturated with a small amount of cold ether to give 5.5 g (73.3% yield) of [3aR-[3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]-hexahydro-4-(4-fluoro-3-hydroxyoctyl)-5-hydroxy-2H-cyclopenta[b]furan-2-one as white crystals: mp 99°-100° C.; [a]D 25 -18.86 (CHCl3, C=1.0).
Anal. Calcd for C15 H25 FO4 : 6, 62.48; H, 8.74. Found: C, 62.48; H, 8.67.
To a solution of 6.0 g (0.0208 mol) of [3aR-[3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]-hexahydro-4-(4-fluoro-3-hydroxy-octyl)-5-hydroxy-2H-cyclopenta[b]furan-2-one dissolved in 100 ml of dry DMF was added 7.2 g of imidazole and 12.9 g of t-butyldimethylchlorosilane. After 18 hr the reaction mixture was poured into 500 ml of 0.5N cold (0° C.) HCl and the mixture extracted with ether. The ether extract was washed with a saturated NaHCO3, solution followed by a saturated NaCl solution. The ether solution was then dried and the solvent removed under reduced pressure. Chromatography on silica gel (2% by volume ethyl acetate/98% by volume hexane -∝ 20% by volume ethyl acetate/80% by volume hexane) afforded 9.5 g (85.4% yield) of [3aR-[3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]-hexahydro-5-[ [(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[[[3-(1,1-dimethylethyl)dimethylsilyl]oxy]-4-fluorooctyl]-2H-cyclopenta[b]furan-2-one; [a]D 25 -30.13 (CHCl3, C=1.08).
Anal. Calcd for C27 H53 FO4 Si2 : C, 62.74; H, 10.34. Found: C, 62.88; H, 10.56.
To a solution of 4.5 ml of diisopropylamine in 50 ml of dry THF (tetrahydrofuran) cooled to 0° C. was added dropwise over a period of twenty minutes 19.6 ml of n-butyllithium (1.5M in hexane). After stirring an additional five minutes at 0° C. the solution was cooled to -40° C. (dry ice/acetone) after which time a solution of 13.1 g (0.0263 mol) of [3aR-[3a alpha,4alpha(3S*),5beta,6a alpha]]-hexahydro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]octyl)-2H-cyclopenta[b]furan-2-one dissolved in 100 ml of THF was added slowly while maintaining the temperature at -40° C. After five minutes at this temperature 4.5 ml of trimethylchlorosilane was added rapidly. The cooling bath was then removed and the reaction allowed to warm to 15° C. The solvent was then removed under vacuum and the residue treated with 50 ml of dry ether. The mixture was then filtered through a cintered glass filter and the solvent evaporated under high vacuum to produce [3aR-[3a alpha,4alpha(3S*),5beta,6a alpha]]-4,5,6,6a-tetrahydro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[3-[[1,1-dimethylethyl)dimethylsilyl]oxy]-octyl]-2-[(trimethylsilyl)oxy]-3aH-cyclopenta[b]furan. This compound was then dissolved at 0° C. in 50 ml of dry CH2 Cl2 containing 5.26 g of KHCO3, followed by the slow addition of 5.0 g of xenon difluoride. The mixture was then stirred for an additional 0.5 hr at 0° C. and then poured into 500 ml of ice water followed by extraction with CH2 Cl2. The organic layer was separated, dried, and the solvent removed under reduced pressure. The residue (9.1 g) was then chromatographed on 500 g of silica gel (2% by volume ethyl acetate/98% by volume petroleum ether to 10% ethyl acetate/90% by volume petroleum ether) and afforded 2.2 g of starting material and 7 g (51.5% yield) of [3S-[3alpha,3a alpha,4alpha(3S*),5beta,6a alpha]]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]octyl]-2H-cyclopenta[b]furan-2-one as a colorless liquid [α]D 25 -29.35 (CHCl3, C=0.726).
Anal. Calcd for C27 H53 FO4 Si2 : C, 62.74; H, 10.34. Found: C, 62.94; H, 10.16.
To a solution of 4.4 g of lithium hexamethyldisilazide in 100 ml of dry THF under argon at -70° C. was added dropwise to a solution of 9.0 g (0.0174 mol) of [3aR-[3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]-hexahydro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[[[3-(1,1-dimethylethyl)dimethylsilyl]oxy]-4-fluorooctyl]-2H-cyclopenta[b]furan-2-one dissolved in 100 ml of dry THF. After stirring for thirty minutes at -70° C. the temperature was allowed to rise to -45° C. at which time 3.8 ml of trimethylchlorosilane was added over a five-minute period. The cooling bath was then removed and the reaction mixture slowly warmed to room temperature. The THF was then removed under high vacuum to produce [3aR-[3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]-4,5,6,6a-tetrahydro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4 -[[[3-(1,1-dimethylethyl)-dimethylsilyl]oxy]-4-fluorooctyl]-3aH-cyclopenta[b]furan as a residue. This residue was dissolved in 100 ml of dry CH2 Cl2 at 0° C. To the solution was then added 3.5 g KHCO3, followed by the slow addition of 3.2 g of xenon difluoride. At the completion of the addition, the reaction mixture was stirred for an additional ten minutes and then poured into a mixture of 250 ml of saturated NaHCO3, containing 1 g of Na2 S2 O3.5H2 O and 500 ml of ether. The aqueous layer was separated and extracted with ether. The ether solutions were combined, washed with a saturated NaCl solution, dried (MgSO4) and the solvent removed under reduced pressure. The residue was then chromatographed on 250 g of silica gel (2% by volume ethyl acetate/98% by volume hexane to 3% by volume ethyl acetate/97% by volume hexane) to give 6.2 g (66.7% yield) of [3S-[3alpha,3a alpha,4alpha(3R*,4S*),-5beta, 6a alpha]]hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)-dimethylsilyl]oxy]-4-[[[3-(1,1-dimethylethyl)dimethylsilyl]oxy]-4-fluorooctyl]-2H-cyclopenta[b]furan-2-one as a colorless oil. [α]D 25 -37.38 (CHCl3, C=0.7).
Anal. Calcd for C27 H52 F2 O4 Si2 : C, 60.63; H, 9.80. Found: C, 60.41; H, 9.60.
To a solution of 7.3 g (0.0141 mol) of [3S-[3alpha,3a alpha,4alpha-(3S*),5beta,6a alpha]]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]octyl]-2H-cyclopenta[b]furan-2-one cooled to -70° C. was added dropwise 14 ml of diisobutylaluminum hydride (25 wt. %, 1.5M) in toluene. The solution was allowed to stir an additional twenty minutes at -70° C. after which time 20 ml of a saturated NH4 Cl solution was added slowly. The mixture was then warmed to 15° C. diluted with 200 ml of ethyl acetate and washed with a saturated NaCl solution. The washings were extracted with ethyl acetate. The ethyl acetate solutions were combined and dried (MgSO4). Removal of the solvent under reduced pressure afforded 7.2 g of residue which was chromatographed over 500 g of silica gel (10% by volume ethyl acetate/90% by volume petroleum ether) to give 6.3 g (86.1% yield) of [3S-[3alpha,3a alpha,4alpha(3S*),5beta,6a alpha]]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]octyl]-2H-cyclopenta[b]furan-2-ol as a colorless oil. [a]D 25 -17.27 (CHCl3, C=0.956).
Anal. Calcd for C27 H55 FO4 Si2 : C, 62.50; H, 10.68. Found: C, 62.16; H, 10.62.
By the procedure of example 8, [3S-[3alpha,3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[[[3-(1,1-dimethylethyl)dimethylsilyl]oxy]-4-fluorooctyl]-2H-cyclopenta[b]-furan-2-one 6.2 g (0.0116 mol) was converted to 6 g (80.6% yield) of [3S-[3alpha,3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[[[3-(1,1-dimethylethyl)dimethylsilyl]oxy]-4-fluorooctyl]2H-cyclopenta[b]furan-2-ol obtained as a colorless oil [a]D 25 -27.38 (CHCl3, C=0.913).
Anal. Calcd for C27 H54 F2 O4 Si2 : C, 60.40; H, 10.14. Found: C, 60.35; H, 9.99.
To a mixture of 15 g (0.0338 mol) of (4-carboxybutyl) triphenylphosphonium bromide (dried under high vaccum at 100° C. for 18 hr) and 13.5 g (0.0736 mol) of sodium hexamethyldi-silazane under argon was added 200 ml of dry THF followed by 13.4 ml of freshly distilled hexamethylphosphoramide. The resulting orange-red suspension was stirred at room temperature for 1 hr. To this mixture was then added 6.3 g (0.0122 mol) of [3S-[3alpha,3a alpha,4alpha(3S*),5beta,6a alpha]]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy-4-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]octyl]-2H-cyclopenta[b]furan-2-ol dissolved in 100 ml of dry THF. The resulting yellow-orange mixture was allowed to stir overnight after which time glacial acetic acid was added dropwise until the mixture became colorless. The mixture was then partitioned between 500 ml of ether and 300 ml of H2 O at 0° C. and then treated with 1N HCl to pH 3. The layers were separated and the water washed with a saturated NaCl solution and dried (MgSO4).
The ether was then removed under reduced pressure to give 15 g of a light yellow oil containing (5Z,7R,9alpha,11alpha,15S)-7-fluoro-11,13-bis-[[(1,1-dimethylethyl)dimethylsilyl]oxy]prost-5-en-1-oic acid. The crude acid was then taken up in 50 ml of dry CH2 Cl2 and treated with an ethereal solution of diazomethane. The excess diazomethane was blown off with a stream of argon. The residue was taken up in ether, dried (MgSO4), and the solvent removed under reduced pressure. Chromatography over 500 g silica gel (2% ethyl acetate/98% by volume petroleum ether to 20% acetate/80% by volume petroleum ether) afforded 5 g of (5Z,7R,9alpha,11alpha,15S)-7-fluoro-11,15-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]prost-5-en-1-oic acid methyl ester.
To a solution of 6.0 g of the methyl ester prepared above in 120 ml of dry acetonitrile was added 16.5 g of N-iodosuccinimide and the resulting mixture stirred 18 hr at room temperature in the absence of light. The mixture was then treated with 500 ml of ether and the resulting solution washed with a 10% by weight aqueous solution of Na2 S2 O3. The washings were back extracted with ether. The ether solutions were combined and dried (MgSO4). The solvent was then removed under reduced pressure to produce a mixture of (5R,6R,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy)-5-iodo-prostanoic acid methyl ester and (5S,6S,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-5-iodo-prostanoic acid methyl ester as a residue. This residue was then treated with a mixture of 60 ml of THF, 120 ml of glacial acetic acid and 60 ml of water. The mixture was warmed to 50° C. for 18 hr and the solvent removed under high vacuum. The residue, 6.7 g was then chromatographed over 500 g. of silica gel (ether to 50% by volume ether/50% by volume ethyl acetate) to afford 2.9 g of a mixture of (5R,6R,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-dihydroxy-5-iodo-prostanoic acid methyl ester and (5S,6S,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,16-dihydroxy-5-iodo-prostanoic acid methyl ester.
Anal, Calcd for C21 H36 FIO5 : C, 49.03; H, 7.05. Found: C, 49.36; H, 7.04.
By the procedure of Example 10, [3S-[3alpha,3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[[[3-(1,1-dimethylethyl)dimethylsilyl]oxy]-4-fluorooctyl]-2H-cyclopenta[b]furan-2-ol 4.6 g (0.0086 mol) was converted to 2 g of a mixture of (5S,6S,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-5-iodo-prostanoic acid methyl ester and (5R,6R,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-5-iodo-prostanoic acid methyl ester via the following intermediates:
(5Z,7R,9alpha,11alpha,15R,16S)-7,16-difluoro-11,15-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-prosta-5-en-1-oic acid,
(5Z,7R,9alpha,11alpha,15R,16S)-7,16-difluoro-11,15-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-prosta-5-en-1-oic acid methyl ester; and
A mixture of (5R,6R,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-bis[[(1,1-dimethyl-ethyl)dimethylsilyl]oxy]-5-iodo-prostanoic acid methyl ester; and (5S,6S,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy-prosta-5-en-1-oic acid methyl ester.
From the mixture produced in Example 11, pure [5S,6S,7beta,9alpha,11alpha,15R,16S]-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-5-iodo-prostanoic acid methyl ester was isolated. [a]D 25 +14.08 (CHCl3, C=0.15).
Anal. Calcd for C21 H35 F2 IO5 : C, 47.38; H, 6.63; Found: C, 46.81; H 6.84.
To a solution of 2.8 g (0.0054 mol) of (5R,6R,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-dihydroxy-5-iodo-prostanoic acid methyl ester and (5S,6S,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-dihydroxy-5-iodoprostanoic acid methyl ester dissolved in 200 ml of dry toluene was added 5.04 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). The solution was then heated under argon at 90° C. for 45 hr. The reaction was then cooled, added to 200 ml of ice water and extracted with 3×250 ml of ether. The ether solutions were combined, washed with a saturated solution of NaCl and dried (MgSO4). The ether was removed under vacuum and the residue (1.9 g) chromatographed over 250 g of silica gel. Elution with 50% by volume ethyl acetate/50% by volume petroleum ether to 75% by volume ethyl acetate/25% by volume petroleum ether afforded 1.2 g of (5Z,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-dihydroxy-prost-5-en-1-oic acid methyl ester as a light yellow oil. [a]D 25 +59.53 (CHCl3, C=0.719).
Anal. Calcd for C21 H35 FO5 : C, 65.26; H, 9.12. Found: C, 64.73; H, 8.95.
Continued elution of the column with 100% by volume of ethyl acetate afforded 0.456 g of (4E,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-dihydroxy-prost-4-en-1-oic acid methyl ester as a light yellow oil.
Anal. Calcd for C21 H35 FO5 : C, 65.26; H, 9.12. Found: C, 64.68; H, 9.13.
A solution of 2 g of a mixture of (5S,6S,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-5-iodo-prostanoic acid methyl ester and (5R,6R,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-5-iodo-prostanoic acid methyl ester and 20 ml of DBU was allowed to stir under an atmosphere of argon for 20 hr. The mixture was then poured into 200 ml of ice water and extracted with ethyl acetate. The ethyl acetate solution was then washed with a saturated NaCl solution and dried (MgSO4). The solvent was then removed under reduced pressure to give 1.7 g of crude product which was chromatographed on 250 grams of silica gel. Elution with 50% by volume ethyl acetate/50% by volume petroleum ether to 75% by volume ethyl acetate and 25% by volume petroleum ether afforded 0.806 g of (5Z,7beta,9alpha,11alpha,15R,16S)-6,9 -epoxy-7,16-difluoro-11,15-dihydroxy-prost-5-en-1-oic-acid methyl ester as a colorless liquid. [a]D 25 +52.85 (CHCl3, C=0.42).
Anal. Calcd for C21 H34 F2 O5 : C, 62.36: H, 8.47. Found: C, 62.04; H, 8.46.
Continued elution with 75% by volume ethyl acetate/25% by volume petroleum ether then afforded 0.497 g of (4E,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-prost-4-en-1-oic acid methyl ester as a colorless oil. [a]D 25 +32.35 (CHCl3, C=0.22).
Anal. Calcd for C21 H34 F2 O5 : C, 62.36; H, 8.47. Found: C, 61.73; H, 8.61.
To a solution of 53.3 mg (0.00013 mol) of (5Z,7beta,9alpha,11alpha,15R,16S)-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-prost--en-1-oic acid methyl ester in 1 ml of CH3 OH, 1 ml of THF and 1 ml H2 O under an atmosphere of argon was added 0.131 ml of 1N NaOH. The reaction mixture was allowed to stir at room temperature for 18 hr and the solvent then removed under high vacuum. The residue was then dissolved in 1 ml of ethyl acetate followed by eight drops of methanol. The mixture was then filtered and the residue washed with a solution of eight drops of methanol in 1 ml of ethyl acetate. To the combined ethyl acetate solutions was added 10 ml of hexane and the mixture allowed to remain in the refrigerator for 18 hr. The solvent was then decanted from the oily residue, and the residue then washed with 10 ml of petroleum ether. The residue was then subjected to high vacuum after which it was dissolved in 4 ml of water and lypolized. The resulting solid was then triturated with hexane and dried under vacuum to give 48 mg of (5Z,7beta,9alpha,11alpha,115R,16S)-6,9-epoxy-7,16-difluoro-11,15-dihydroxy-prost--en-1-oic acid sodium salt as a white crystalline solid.
Anal. Calcd for C20 H31 F2 NaO5 : C, 58.24; H, 7.58; F, 9.21. Found: C, 57.54; H, 7.44; F, 9.88.
By the procedure of Example 15, 50 mg of (5Z,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,15-dihydroxy-prost-5-en-1-oic acid methyl ester was converted to 26 mg of (5Z,7beta,9alpha,11alpha,15S)-6,9-epoxy-7-fluoro-11,16-dihydroxyprost-5-en-1-oic acid monosodium salt monohydrate (obtained as a white solid).
Anal. Calcd for C20 H32 F2 NaO5.H2 O: C, 58.24; H, 8.31; F. 4.61. Found: C, 58.04; H, 8.43; F, 4.45.
______________________________________ Ingredient mg/cap ______________________________________ 1. [5Z,7beta,9alpha, 0.01 0.5 5.0 25.0 11alpha,15R,16S]- 6,9-epoxy-7,16-di- fluoro-11,15-dihydroxy prosten-5-en-1-oic acid sodium salt 2. Lactose Hydrose 168.99 168.5 159.0 123.0 3. Corn Starch 20.0 20.0 25.0 35.0 4. Talc 10.0 10.0 10.0 15.0 5. Mg stearate 1.0 1.0 1.0 2.0 200.0 200.0 200.0 200.0 ______________________________________ Manufacturing Procedure ______________________________________ 1. Mix items 1, 2, and 3 in a suitable mixer for 30 minutes. 2. Add items 4 and 5 and mix for 3 minutes. 3. Fill in suitable capsule. ______________________________________
______________________________________ Ingredient mg/cap ______________________________________ 1. (5Z,7beta,9alpha, 0.01 0.5 5.0 25.0 11alpha,15R,16S)- 6,9-epoxy-7-fluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester 2. Lactose Hydrose 168.99 168.5 159.0 123.0 3. Corn Starch 20.0 20.0 25.0 35.0 4. Talc 10.0 10.0 10.0 15.0 5. Mg stearate 1.0 1.0 1.0 2.0 200.0 200.0 200.0 200.0 ______________________________________ Manufacturing Procedure ______________________________________ 1. Mix items 1, 2, and 3 in a suitable mixer for 30 minutes. 2. Add items 4 and 5 and mix for 3 minutes. 3. Fill in suitable capsule. ______________________________________
______________________________________ Ingredient mg/cap ______________________________________ 1. (5Z,7beta,9alpha, 0.01 0.5 5.0 25.0 11alpha,15R,16S)- 6,9-epoxy-7,16-difluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester 2. Lactose Hydrose 168.99 168.5 159.0 123.0 3. Corn Starch 20.0 20.0 25.0 35.0 4. Talc 10.0 10.0 10.0 15.0 5. Mg stearate 1.0 1.0 1.0 2.0 200.0 200.0 200.0 200.0 ______________________________________ Manufacturing Procedure ______________________________________ 1. Mix items 1, 2, and 3 in a suitable mixer for 30 minutes. 2. Add items 4 and 5 and mix for 3 minutes. 3. Fill in suitable capsule. ______________________________________
______________________________________ Ingredient mg/cap ______________________________________ 1. [5Z,7beta,9alpha, 0.01 0.5 5.0 25.0 11alpha,15R,16S]- 6,9-epoxy-7,16-di- fluoro-11,15-dihydroxy prosten-5-en-1-oic acid sodium salt 2. PEG 400 149.49 149.0 194.5 374.5 (polyethylene glycol molecule at 400) 3. Ascorbyl Palmitate 0.5 0.5 0.5 0.5 150.0 150.0 200.0 400.0 ______________________________________ Manufacturing Procedure ______________________________________ 1. Dissolve item 3 in item 2. 2. Add item 1 to the solution in Step 1 and mix until dissolved. 3. Fill in soft gelatin capsule. ______________________________________
______________________________________ Ingredient mg/cap ______________________________________ 1. (5Z,7beta,9alpha, 0.01 0.5 5.0 25.0 11alpha,15R,16S)- 6,9-epoxy-7,16-difluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester 2. PEG 400 149.49 149.0 194.5 374.5 3. Ascorbyl Palmitate 0.5 0.5 0.5 0.5 150.0 150.0 200.0 400.0 ______________________________________ Manufacturing Procedure ______________________________________ 1. Dissolve item 3 in item 2. 2. Add item 1 to the solution in Step 1 and mix until dissolved. 3. Fill in soft gelatin capsule. ______________________________________
______________________________________ Ingredient mg/cap ______________________________________ 1. [5Z,7beta,9alpha, 0.01 0.5 5.0 25.0 11alpha,15R,16S]- 6,9-epoxy-7,16-di- fluoro-11,15-dihydroxy prosten-5-en-1-oic acid sodium salt 2. Lactose anhydrose 106.99 106.5 102.0 118.0 DTG 3. Avicel pH 102 15.0 15.0 15.0 25.0 (microcrystalline cellulose) 4. Modified Starch 7.0 7.0 7.0 10.0 5. Magnesium stearate 1.0 1.0 1.0 2.0 130.0 130.0 130.0 130.0 ______________________________________ Manufacturing Procedure ______________________________________ 1. Dissolve item 1 in a suitable solvent such as alcohol. 2. Spread the solution in Step 1 over item 2, dry. 3. Add items 3 and 4 and mix for 10 minutes. 4. Add magnesium stearate and mix for 3 minutes and compress ______________________________________
______________________________________ Ingredient mg/cap ______________________________________ 1. (5Z,7beta,9alpha, 0.01 0.5 5.0 25.0 11alpha,15R,16S)- 6,9-epoxy-7,16-difluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester 2. Lactose Anhydrous 106.99 106.5 102.0 118.0 3. Avicel pH 102 15.0 15.0 15.0 25.0 4. Modified starch 7.0 7.0 7.0 10.0 5. Magnesium stearate 1.0 1.0 1.0 2.0 130.0 130.0 130.0 130.0 ______________________________________ Manufacturing Procedure ______________________________________ 1. Dissolve item 3 in item 2. 2 Add item 1 to the solution in Step 1 and mix until dissolved. 3. Fill in soft gelatin capsule. ______________________________________
______________________________________ Ingredient mg/cap ______________________________________ 1. [5Z,7beta,9alpha, 0.01 0.5 5.0 25.0 11alpha,15R,16S]- 6,9-epoxy-7,16-di- fluoro-11,15-dihydroxy prosten-5-en-1-oic acid sodium salt 2. Lactose 101.99 101.5 97.0 118.0 Anhydrous DTG.sup.(a) 3. Avicel pH 102 20.0 20.0 20.0 25.0 4. Modified starch 7.0 7.0 7.0 10.0 5. Magnesium stearate 1.0 1.0 1.0 2.0 130.0 130.0 130.0 130.0 ______________________________________ Manufacturing Procedure ______________________________________ 1. Prepare a premix of item 1 with part of item 2. 2. Add the mixture in Step 1 to the mixture of remainder of items 2, 3 and 4 and mix for 10 minutes. Add item 5 and mix for 3 minutes; compress using suitable punch on suitable press. ______________________________________
______________________________________ Ingredient mg/cap ______________________________________ 1. (5Z,7beta,9alpha, 0.01 0.5 5.0 25.0 11alpha,15R,16S)- 6,9-epoxy-7,16-difluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester 2. Lactose Anhydrous 101.99 101.5 97.0 118.0 DTG 3. Avicel pH 102 20.0 20.0 20.0 25.0 4. Modified starch 7.0 7.0 7.0 10.0 5. Magnesium stearate 1.0 1.0 1.0 2.0 130.0 130.0 130.0 180.0 ______________________________________ Manufacturing Procedure ______________________________________ 1. Prepare a premix of item 1 with part of item 2. 2. Add the mixture in Step 1 to the mixture of remainder of items 2, 3 and 4 and mix for 10 minutes. Add item 5 and mix for 3 minutes: compress using suitable punch on suitable press. ______________________________________
______________________________________ The following is the quantitative composition of drug: Reasonable Ingredients g/kg Variations ______________________________________ (5Z,7beta,9alpha, 0.525* -- 11alpha,15R,16S)- 6,9-epoxy-7,16-difluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester Glyceryl Monostearate S.E..sup.1 100.00 80-120 Polysorbate 60.sup.2 20.00 15-25 Cetyl Alcohol 50.00 40-60 Petrolatum 70.00 50-90 Methyl Paraben 1.50 1.25-1.75 Propyl Paraben 0.50 0.4-0.6 Propylene Glycol 200.00 150-250 Purified Water 574.055 525-625 Total 1016.58 gm ______________________________________ .sup.1 Arlacel l65 .sup.2 Tween 60 *3% excess of drug
______________________________________ The followinq is the quantitative composition of drug: Reasonable Ingredients g/kg Variations ______________________________________ (5Z,7beta,9alpha,11alpha,- 0.525* -- 15R,16S)-6,9-epoxy-7-fluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester Glyceryl Monostearate S.E..sup.1 100.00 80-120 Polysorbate 60.sup.2 20.00 15-25 Cetyl Alcohol 50.00 40-60 Petrolatum 70.00 50-90 Methyl Paraben 1.50 1.25-1.75 Propyl Paraben 0.50 0.4-0.6 Propylene Glycol 200.00 150-250 Purified Water 574.055 525-625 Total 1016.58 gm ______________________________________ .sup.1 Arlacel 165 .sup.2 Tween 60 *3% excess of drug
______________________________________ The following is the quantitative composition of drug: Reasonable Ingredients g/kg Variations ______________________________________ (5Z,7beta,9alpha, 2.575* -- 11alpha,15R,16S)- 6,9-epoxy-7,16-difluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester Glyceryl Monostearate S.E..sup.1 100.00 80-120 Polysorbate 60.sup.2 20.00 15-25 Cetyl Alcohol 50.00 40-60 Petrolatum 70.00 50-90 Methyl Paraben 1.50 1.25-1.75 Propyl Paraben 0.50 0.4-0.6 Propylene Glycol 200.00 150-250 Purified Water 571.395 500-600 Total 1015.97 gm ______________________________________ .sup.1 Arlacel 165 .sup.2 Tween 60 *3% excess of drug
______________________________________ The following is the quantitative composition of drug: Reasonable Ingredients g/kg Variations ______________________________________ (5Z,7beta,9alpha, 11alpha,- 2.575* -- 15R,16S)-6,9-epoxy-7-fluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester Glyceryl Monostearate S.E..sup.1 100.00 80-120 Polysorbate 60.sup.2 20.00 15-25 Cetyl Alcohol 50.00 40-60 Petrolatum 70.00 50-90 Methyl Paraben 1.50 1.25-1.75 Propyl Paraben 0.50 0.4-0.6 Propylene Glycol 200.00 150-250 Purified Water 571.395 500-600 Total 1015.97 gm ______________________________________ .sup.1 Arlacel 165 .sup.2 Tween 60 *3% excess of drug
______________________________________ The following is the quantitative composition of drug: Reasonable Ingredients g/kg Variations ______________________________________ [5Z,7beta,9alpha, 5.150* -- 11alpha,15R,16S]- 6,9-epoxy-7,16-di- fluoro-11,15-dihydroxy prosten-5-en-1-oic acid sodium salt Glyceryl Monostearate S.E..sup.1 100.00 80-120 Polysorbate 60.sup.2 20.00 15-25 Cetyl Alcohol 50.00 40-60 Petrolatum 70.00 50-90 Methyl Paraben 1.50 1.25-1.75 Propyl Paraben 0.50 0.4-0.6 Propylene Glycol 200.00 150-250 Purified Water 568.05 500-600 Total 1015.20 gm ______________________________________ .sup.2 Arlacel 165 .sup.2 Tween 60 *3% excess of drug
______________________________________ The following is the quantitative composition of drug: Reasonable Ingredients g/kg Variations ______________________________________ (5Z,7beta,9alpha, 11alpha,- 5.150* -- 15R,16S)-6,9-epoxy-7-fluoro- 11,15-dihydroxy prost-5-en-1-oic acid methyl ester Glyceryl Monostearate S.E..sup.1 100.00 80-120 Polysorbate 60.sup.2 20.00 15-25 Cetyl Alcohol 50.00 40-60 Petrolatum 70.00 50-90 Methyl Paraben 1.50 1.25-1.75 Propyl Paraben 0.50 0.4-0.6 Propylene Glycol 200.00 150-250 Purified Water 568.05 475-575 Total 1015.20 gm ______________________________________ .sup.1 Arlacel 165 .sup.2 Tween 60 *3% excess of drug
Claims (8)
1. A compound of the formula: ##STR9## wherein R2 is hydrogen, methyl or fluoro, R2 ' is fluoro, hydrogen, trifluoromethyl, or methyl; R5 is tri(lower alkyl)silyl; with the proviso that when R2 ' is trifluoromethyl, R2 is hydrogen or methyl;
optical antipodes or racemates thereof.
2. The compound of claim 1 which is [3S-[3alpha,3a alpha,4alpha(3S*),5beta,6a alpha]]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl)oxy]-4-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]octyl]-2H-cyclopenta[b]furan-2-ol.
3. The compound of claim 1 which is [3S-[3alpha,3a alpha,4alpha(3R*,4S*),5beta,6a alpha)]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[[[3-(1,1-dimethylethyl)dimethylsilyl]oxy]-4-fluorooctyl]-2H-cyclopenta[b]furan-2-ol.
4. A compound of the formula: ##STR10## wherein R2 is methyl, hydrogen or fluoro; R2 ' is fluoro, hydrogen, trifluoromethyl or methyl; R5 is tri(lower alkyl silyl); and with the proviso that when R2 ' is trifluoromethyl, R2 is hydrogen or methyl;
optical antipodes and racemates thereof.
5. The compound of claim 4 which is [3S-[3alpha,3a alpha,4alpha(3S*),5beta,6a alpha]]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]]oxy-4-[[[3-(1.1-dimethylethyl)dimethylsilyl]oxy]octyl]-2H-cyclopenta[b]furan-2-one.
6. The compound of claim 4 which is [3S-[3alpha,3a alpha,4alpha(3R*,4S*),5beta,6a alpha]]-hexahydro-3-fluoro-5-[[(1,1-dimethylethyl)dimethylsilyl]]oxy]-4-[[[3-(1,1-dimethylethyl)dimethylsilyl]oxy]-4-fluorooctyl]-2H-cyclopenta[b]furan-2-one.
7. A compound of the formula: ##STR11## wherein R5 and R7 are tri(lower alkyl)silyl; R2 ' is fluoro, hydrogen, trifluoromethyl, or methyl; R2 is hydrogen, methyl or fluoro; with the proviso that when R2 ' is trifluoromethyl, R2 is hydrogen or methyl,
optical antipodes and racemates thereof.
8. The compound of claim 1 which is [3aR-[3a alpha,4alpha(3R*),5beta,6a alpha]]-4,5,6,6a-tetrahydro-5-[[1,1-dimethylethyl)dimethylsilyl]oxy]-4-[3-[1,1-dimethylethyl)dimethylsilyl]oxy]-octyl-2-[(trimethylsilyl)oxy]-3aH-cyclopenta[b]furan.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US06/885,993 US4680415A (en) | 1985-06-24 | 1986-09-08 | Intermediates for 7-fluoro dihydro PGI compounds |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/747,740 US4634782A (en) | 1985-06-24 | 1985-06-24 | 7-fluoro-dihydro PGI compounds |
US06/885,993 US4680415A (en) | 1985-06-24 | 1986-09-08 | Intermediates for 7-fluoro dihydro PGI compounds |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US06/747,740 Division US4634782A (en) | 1985-06-24 | 1985-06-24 | 7-fluoro-dihydro PGI compounds |
Publications (1)
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US4680415A true US4680415A (en) | 1987-07-14 |
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US06/885,993 Expired - Fee Related US4680415A (en) | 1985-06-24 | 1986-09-08 | Intermediates for 7-fluoro dihydro PGI compounds |
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US (1) | US4680415A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040249172A1 (en) * | 2001-05-24 | 2004-12-09 | Greenwood Alan Kenneth | Process for the preparationof prostaglandins and analogues thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2088856A (en) * | 1980-10-27 | 1982-06-16 | Chinoin Gyogyszer Es Vegyeszet | 7-substituted pg12-derivatives their preparation and pharmaceutical compositions containing them |
EP0054795A2 (en) * | 1980-12-09 | 1982-06-30 | Teijin Limited | Novel halogenated prostacyclins, process for the production thereof, and pharmaceutical use thereof |
GB2094310A (en) * | 1981-03-11 | 1982-09-15 | Hoffmann La Roche | Novel fluoro-prostacyclins |
EP0148953A1 (en) * | 1983-06-10 | 1985-07-24 | Asahi Glass Company Ltd. | 7-fluoroprostaglandins and process for their preparation |
US4558142A (en) * | 1981-03-11 | 1985-12-10 | Hoffmann-La Roche Inc. | 7-Fluoro-prostacyclin analogs |
-
1986
- 1986-09-08 US US06/885,993 patent/US4680415A/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2088856A (en) * | 1980-10-27 | 1982-06-16 | Chinoin Gyogyszer Es Vegyeszet | 7-substituted pg12-derivatives their preparation and pharmaceutical compositions containing them |
EP0054795A2 (en) * | 1980-12-09 | 1982-06-30 | Teijin Limited | Novel halogenated prostacyclins, process for the production thereof, and pharmaceutical use thereof |
GB2094310A (en) * | 1981-03-11 | 1982-09-15 | Hoffmann La Roche | Novel fluoro-prostacyclins |
US4558142A (en) * | 1981-03-11 | 1985-12-10 | Hoffmann-La Roche Inc. | 7-Fluoro-prostacyclin analogs |
EP0148953A1 (en) * | 1983-06-10 | 1985-07-24 | Asahi Glass Company Ltd. | 7-fluoroprostaglandins and process for their preparation |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040249172A1 (en) * | 2001-05-24 | 2004-12-09 | Greenwood Alan Kenneth | Process for the preparationof prostaglandins and analogues thereof |
US20050261374A1 (en) * | 2001-05-24 | 2005-11-24 | Resolution Chemicals Limited | Process for the preparation of prostaglandins and analogues thereof |
US20050272877A1 (en) * | 2001-05-24 | 2005-12-08 | Resolution Chemicals Limited | Process for the preparation of prostaglandins and analogues thereof |
US7268239B2 (en) * | 2001-05-24 | 2007-09-11 | Resolution Chemicals Limited | Process for the preparation of prostaglandins and analogues thereof |
AU2002321396B2 (en) * | 2001-05-24 | 2007-10-18 | Resolution Chemicals Limited | Process for the preparation of prostaglandins and analogues thereof |
US7498458B2 (en) | 2001-05-24 | 2009-03-03 | Resolution Chemicals Limited | Process for the preparation of prostaglandins and analogues thereof |
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